Tag | Content |
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EnhancerAtlas ID | HS145-07816 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr14:101539400-101540160 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr14:101539709-101539722 | ATGACATCATTAC | - | 6.48 | JUND(var.2) | MA0492.1 | chr14:101539708-101539723 | AATGACATCATTACC | - | 6.2 | NR2C2 | MA0504.1 | chr14:101539588-101539603 | AGGGGGCAGAGGCCA | + | 6.05 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I101070 | chr14 | 101537262 | 101542129 |
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Enhancer Sequence | AGGGAGCAAC CTCCTGAAGT CGGGGCTCAC TCCTGGGTCC CCCTCCACTG CATGCGAGCC 60 CCCCGTTCCA AGGCAGGAGC CAGGGTCACG AAAATGCATG CTTCTTCATC AATCCGAGGT 120 CTCAAACGGC TCCCCCAGCC CCACTGCCTG CCCGTTCCAG GCCTGGGGCT GGCAGCCTGG 180 GCCCCACGAG GGGGCAGAGG CCAGAGCCCG GCGGCAGAGC CCGTGCCCAC GCCTCGCTGC 240 TGCCAGCCTC CGCTTGGTCA CGACACAGCC AGGCTGACTC AGACACAGCC CCAAGCGGGA 300 GCCTCATAAA TGACATCATT ACCTATGAAA CCTGCCGTGT AGTGCGCTAG CAGGGAAGGA 360 CACACTCTGG CCGCCCGGTG ACTCACACTG TTTTCCCCAG AGCCTTCCTG CTCCACCGCC 420 TGGGTCTGAG CTGGCTGGGC AGGGGGAGGG GGCACTCAGC TTGGCCTCAC TCCCCCGCTC 480 TGCTGCAAAT GCAAAAGCAA TCGGCCAGGC AGCCACCATC CTGCTGAGGG CTGTGTGTGG 540 GGGTGGCGGG GAGGAGGGGG GGCACCATCT CTCCGGCCTC CCTCTGCAGC CCCAGTGGCG 600 CTCCAGAGGG ACTGTCAGTT GCCTATGACA GGGGAGGAAA CTGAGGCCTA AAGAGGCCCA 660 ATGCCTGGCC TCACAGATCC CACAGGGGAG GGTGGCTTCG GCTCATGCTG GGAACCCCCA 720 GGGAGACCCT TCGGCGAACC CAGCCGCTGG GCAAAGCTGC 760
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